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1,000 results • Page
4 of 20
Sort: Views
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Views
Votes
Replies
15
votes
7
replies
19k
views
using featureCounts in command line
featureCounts
updated 11 months ago by
Adyasha
• 0 • written 8.6 years ago by
zizigolu
★ 4.3k
83
votes
20
replies
19k
views
17 follow
How Do Pathway Databases Compare?
pathway
database
subjective
updated 9 months ago by
Peter Karp
▴ 30 • written 13.5 years ago by
Shigeta
▴ 470
39
votes
6
replies
19k
views
Tutorial:
Creating chromosome karyotype plot with R and ggplot2
ggplot2
R
chromosome
karyotype
updated 11 months ago by
Ram
43k • written 6.6 years ago by
steve
★ 3.5k
28
votes
11
replies
19k
views
9 follow
Salary For A Bioinformatics Programmer In Europe?
career
updated 11 months ago by
Ram
43k • written 12.6 years ago by
Jeroen Van Goey
2.3k
24
votes
15
replies
19k
views
7 follow
how can I remove duplicated variants from vcf file?
SNP
vcf
updated 8 months ago by
Ram
43k • written 6.7 years ago by
kk.mahsa
▴ 140
14
votes
17
replies
19k
views
6 follow
HISAT2 command help
RNA-Seq
alignment
updated 3 months ago by
DareDevil
★ 4.3k • written 8.2 years ago by
dina.hesham139
▴ 170
38
votes
21
replies
19k
views
8 follow
Tool:
pybam - 100% python BAM reader
python
htspython
bam
pysam
updated 10 months ago by
Ram
43k • written 8.0 years ago by
John
13k
20
votes
16
replies
19k
views
6 follow
Conversion of Gene Name to Ensembl ID
gene
RNA-Seq
R
genome
updated 5 months ago by
Nat.Nataren
▴ 10 • written 4.1 years ago by
bazok
▴ 20
28
votes
7
replies
19k
views
6 follow
VCF merge or concatenate?
snp
VCF
VCFTools
written 4.8 years ago by
rokragna295
▴ 60
8
votes
6
replies
19k
views
Converting gtf format to bed format
bed
updated 3 months ago by
Apex92
▴ 280 • written 9.5 years ago by
thjnant
▴ 160
176
votes
46
replies
19k
views
26 follow
Forum:
Crac: Funny And/Or Weird Names For Bioinformatics Tools
humor
5 months ago by
Istvan Albert
100k
26
votes
9
replies
19k
views
8 follow
Favorite Splice Site Prediction/Evaluation Tools
splicing
prediction
updated 10 months ago by
abhilashdasari.10
▴ 30 • written 11.4 years ago by
Alex Paciorkowski
3.5k
83
votes
34
replies
19k
views
22 follow
Tutorial:
Enrichment Analysis, Clustering and Scoring with pathfindR
enrichment
R
pathway
active-subnetwork
updated 10 months ago by
adelheidkratzer
• 0 • written 5.8 years ago by
egeulgen
★ 1.3k
38
votes
26
replies
18k
views
16 follow
GO analysis: DAVID vs GREAT vs GOrilla
RNA-Seq
ChIP-Seq
GO
gene ontology
written 8.2 years ago by
biostart
▴ 370
15
votes
9
replies
18k
views
8 follow
How to count fasta sequences efficiently using (or not ) biopython
biopython
python
fasta
updated 5 months ago by
Mark
★ 1.5k • written 6.2 years ago by
juan.crescente
▴ 110
3
votes
8
replies
18k
views
Downloading gtf file for RefSeq
RNA-Seq
RefSeq
GTF
updated 3 months ago by
xiaoleiusc
▴ 140 • written 6.6 years ago by
KVC_bioinfo
▴ 590
13
votes
7
replies
18k
views
Running STAR aligner on paired-end reads as single-end read
RNA-Seq
paired end
single end
STAR
align
updated 4 months ago by
xiaoleiusc
▴ 140 • written 5.7 years ago by
Glory Basumata
▴ 140
6
votes
5
replies
18k
views
7 follow
How different is rlog transformation from vst transformation in DESeq2
DESeq2
count normalization
updated 8 months ago by
ATpoint
81k • written 5.6 years ago by
piyushjo
▴ 700
51
votes
6
replies
18k
views
Decoy In Reference Assembly
1000genomes
updated 11 months ago by
kmzhou4
• 0 • written 10.9 years ago by
Sangwoo Kim
▴ 420
13
votes
13
replies
18k
views
9 follow
How Do I Translate Multiple (More Than 25000) Dna Sequences With Different Frames To Protein Seuquence?
dna
protein
updated 11 days ago by
ummeswaiba
• 0 • written 10.3 years ago by
biostar
▴ 170
38
votes
12
replies
18k
views
8 follow
BEDOPS gtf2bed conversion error with Ensembl GTF
gtf2bed
ensembl
bedops
gtf
updated 7 weeks ago by
Alex Reynolds
35k • written 7.7 years ago by
bioinformatics.cancer
▴ 260
1
vote
2
replies
18k
views
Forum:
Would you rather analyze a dataset with a strong, non-collinear batch effect, or a weak, collinear batch effect.
collinear
latent
batch-effect
variable
GLM
8 months ago by
LauferVA
4.2k
17
votes
10
replies
18k
views
Regarding Split reads and discordant reads
genome
sequence
sequencing
alignment
updated 11 months ago by
Ram
43k • written 6.5 years ago by
DL
▴ 50
6
votes
9
replies
18k
views
HISAT2 software installation
RNA-Seq
updated 10 weeks ago by
GenoMax
141k • written 6.6 years ago by
saj98
▴ 140
12
votes
11
replies
17k
views
Trying to get genome for bedtools
genome
updated 8 months ago by
mg
▴ 250 • written 7.7 years ago by
radwa.raed
▴ 40
21
votes
11
replies
17k
views
the problem with rpkm (and tpm)
RNA-Seq
next-gen
gene-expression
normalization
updated 9 months ago by
Chris
▴ 260 • written 9.5 years ago by
user123456
▴ 180
65
votes
24
replies
17k
views
14 follow
Mapping Snps To Pathways
snp
genotyping
pathway
gene
enrichment
updated 6 months ago by
Ram
43k • written 14.1 years ago by
Pierre Lindenbaum
161k
8
votes
6
replies
17k
views
News:
Bioinformatics PhD Programs in the US
education
PhD
updated 11 months ago by
Ram
43k • written 6.4 years ago by
Ahmed Youssef
▴ 70
9
votes
10
replies
17k
views
8 follow
Forum:
Open Source Bioinformatics projects for beginners
Open-Source
Beginners
updated 11 weeks ago by
Saransh
• 0 • written 6.2 years ago by
Eugenia84
▴ 40
20
votes
10
replies
17k
views
Could you please explain Fold change, % of change, and log2 fold change (L2FC) to a layment?
gene
RNA-Seq
next-gen
fold-change
updated 7 months ago by
Ram
43k • written 4.5 years ago by
WUSCHEL
▴ 750
17
votes
9
replies
17k
views
6 follow
Tool:
ggrepel: repel overlapping text labels in ggplot2
R
visualization
updated 10 months ago by
Ram
43k • written 8.3 years ago by
Kamil
★ 2.3k
3
votes
9
replies
16k
views
8 follow
Module to RMSD two proteins with Python?
python
protein-structure
updated 9 months ago by
Aleksandr
• 0 • written 8.3 years ago by
bef1
• 0
12
votes
11
replies
16k
views
10 follow
Retrieve The Reads And Fastq From Bam File
samtools
updated 6 months ago by
Reem
• 0 • written 11.5 years ago by
rehma.ar
▴ 290
35
votes
17
replies
16k
views
12 follow
Tutorial:
Machine Learning For Cancer Classification - Part 3 - Predicting With A Random Forest Classifier
machine-learning
classification
updated 11 months ago by
GenoMax
141k • written 10.4 years ago by
Obi Griffith
20k
10
votes
8
replies
16k
views
6 follow
Error: Eof Marker Is Absent When Processing A Bam File
samtools
updated 11 months ago by
Ram
43k • written 11.6 years ago by
Mary
▴ 50
27
votes
6
replies
16k
views
Tool:
Bioawk - Fasta, Fastq, Sam, Bed, Gff Aware Awk Programming
awk
updated 9 months ago by
Ram
43k • written 11.8 years ago by
Istvan Albert
100k
30
votes
18
replies
16k
views
8 follow
Is It Possible For Two Different Affymetrix Probe Set Id To Have Common Annotations To Same Gene ?
microarray
annotation
affymetrix
probeset
updated 5 months ago by
Ram
43k • written 14.1 years ago by
Khader Shameer
18k
21
votes
6
replies
16k
views
survfit(Surv()) P-value interpretation for 3 survival curves?
survfit
Surv
survival curves
R
updated 26 days ago by
marshelma
• 0 • written 4.5 years ago by
JJDollar
▴ 130
47
votes
15
replies
16k
views
10 follow
DESeq2 compare all levels
differential-gene-expression
RNA-Seq
DESeq2
updated 4 weeks ago by
Bionaught
• 0 • written 5.8 years ago by
firestar
★ 1.6k
7
votes
11
replies
16k
views
11 follow
How to generate KEGG pathway classification chart
RNA-Seq
kegg
updated 9 months ago by
microecologist93
▴ 20 • written 5.1 years ago by
dongchenchen
▴ 30
35
votes
10
replies
16k
views
11 follow
Which Chip Seq Peak Callers Do You Use?
chip-seq
peak-calling
updated 5 months ago by
Ram
43k • written 14.0 years ago by
Stew
★ 1.4k
15
votes
34
replies
16k
views
10 follow
Issues installing bcl2fastq?
bcl2fastq
demultiplexing
updated 6 weeks ago by
barslmn
★ 2.1k • written 6.7 years ago by
a.rex
▴ 350
21
votes
7
replies
16k
views
6 follow
GFA to Fasta file
sequence
updated 3 months ago by
Adam Taranto
▴ 40 • written 8.4 years ago by
marcela.uliano
▴ 90
7
votes
14
replies
16k
views
7 follow
Tool:
Art: Simulation Tools To Generate Synthetic Next-Generation Sequencing Reads.
sequence
updated 9 months ago by
Ram
43k • written 11.8 years ago by
Istvan Albert
100k
68
votes
25
replies
16k
views
12 follow
Tool:
sra-explorer : find SRA and FastQ download URLs in a couple of clicks
fastq
SRA
updated 5 months ago by
GenoMax
141k • written 5.1 years ago by
Phil Ewels
★ 1.4k
28
votes
4
replies
15k
views
Tool:
Plotting GSEA output in R
RNA-Seq
javaGSEA
GSEA
updated 10 months ago by
Ram
43k • written 7.7 years ago by
thomaskuilman
▴ 850
15
votes
11
replies
15k
views
10 follow
TCGA/Broad Institute CNV Files Segment Mean
tcga
cnv
updated 4 months ago by
sativus
▴ 20 • written 9.6 years ago by
dirigible2012
▴ 320
12
votes
10
replies
15k
views
6 follow
conversion of GFF3 formate to BED format
RNA-Seq
updated 10 weeks ago by
Ram
43k • written 5.8 years ago by
blooming.daisy333
▴ 110
9
votes
13
replies
15k
views
Sort bam file by coordinates using samtools
next-gen-sequencing
gene
rna-seq
updated 10 months ago by
Ram
43k • written 5.6 years ago by
Shahzad
▴ 30
49
votes
18
replies
15k
views
12 follow
What Phylogeny Viewing Software Do You Use?
software
phylogenetics
visualization
updated 5 months ago by
Ram
43k • written 14.1 years ago by
Roderic Page
▴ 390
1,000 results • Page
4 of 20
Recent Votes
Comment: featureCounts --primary tag counting uniquely mapped reads and excludes multi-ma
Answer: Duplicate marking, read names, and the SRA
Comment: Installing/switching between versions of R/Rstudio/Bioconductor
Comment: Installing/switching between versions of R/Rstudio/Bioconductor
Comment: Installing/switching between versions of R/Rstudio/Bioconductor
Answer: Cellranger count error: Input FASTQ file ended prematurely
Comment: Load a full GFF3 into annotation track using arrow (Apollo)
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> so a single Rscript could utilise multiple environments and versions How is that sane, let alone "better"? Also, why use `snap` for curl…
Comment: how to find genes that are significantly expressed in brain cortex samples
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Normalized how?
Comment: Duplicate marking, read names, and the SRA
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141k
With public data one has to work with what is there. If the information about position is absent then only thing that could be done is to l…
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Comment: what's the genomic location and name of gene responsible for orange and black pa
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If GPT is right then it says that: > The specific gene responsible for the orange and non-orange (black or > gray) fur colors in cats is t…
Comment: what's the genomic location and name of gene responsible for orange and black pa
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Jean-Karim Heriche
27k
As far as I know the Orange locus hasn't been mapped to a gene. Maybe this paper will help in narrowing the search: https://www.ncbi.nlm.ni…
Comment: Duplicate marking, read names, and the SRA
by
Luka
• 0
>Curios if there a reference for this? [Apparently it's not deprecated yet][1], but will be soon and the SRA intends for it to be at some …
Comment: Installing/switching between versions of R/Rstudio/Bioconductor on personal mach
by
Ram
43k
I prefer RStudio for new projects as well. The moment I need versions though, RStudio becomes a burden. I wish one could launch RStudio fro…
Comment: what's the genomic location and name of gene responsible for orange and black pa
by
GenoMax
141k
According to ChatGPT: The gene responsible for the orange and black patches of fur in calico cats (and tortoiseshell cats) is the X-linked …
Comment: Installing/switching between versions of R/Rstudio/Bioconductor on personal mach
by
BioinfGuru
★ 1.7k
Certainly true. Switching versions is way simpler that way, at the cost of the familiarity of the Rstudio IDE - especially if the code is w…
Comment: Duplicate marking, read names, and the SRA
by
GenoMax
141k
> fastq-dump is deprecated Curios if there a reference for this? `fasterq-dump` seems to allow for parallel streams but `fastq-dump` is st…
Comment: Duplicate marking, read names, and the SRA
by
Luka
• 0
>In many cases those remain recoverable using the -F option when you dump the data (cloud download not required) The -F option (or any equ…
Answer: Duplicate marking, read names, and the SRA
by
GenoMax
141k
To be specific, not every dataset in SRA loses the original identifiers. In many cases those remain recoverable using the `-F` option when …
Comment: Installing/switching between versions of R/Rstudio/Bioconductor on personal mach
by
Ram
43k
To use different versions of R and bioconductor, you don't really need RStudio. One can simply create new conda environments with the requi…
Comment: Installing/switching between versions of R/Rstudio/Bioconductor on personal mach
by
BioinfGuru
★ 1.7k
Done. Thank you.
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